EP1679308A4 - Novel indazole derivative - Google Patents

Novel indazole derivative

Info

Publication number
EP1679308A4
EP1679308A4 EP04792805A EP04792805A EP1679308A4 EP 1679308 A4 EP1679308 A4 EP 1679308A4 EP 04792805 A EP04792805 A EP 04792805A EP 04792805 A EP04792805 A EP 04792805A EP 1679308 A4 EP1679308 A4 EP 1679308A4
Authority
EP
European Patent Office
Prior art keywords
alkyl
hydrogen
halogeno
aryloxy
alkoxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP04792805A
Other languages
German (de)
French (fr)
Other versions
EP1679308B1 (en
EP1679308A1 (en
Inventor
Masahiko Hagihara
Ken-Ichi Komori
Hidetoshi Sunamoto
Hiroshi Nishida
Takeshi Matsugi
Tadashi Nakajima
Masakazu Hatano
Kazutaka Kido
Hideaki Hara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ube Corp
Original Assignee
Santen Pharmaceutical Co Ltd
Ube Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Santen Pharmaceutical Co Ltd, Ube Industries Ltd filed Critical Santen Pharmaceutical Co Ltd
Priority to EP12160543.0A priority Critical patent/EP2468729B1/en
Publication of EP1679308A1 publication Critical patent/EP1679308A1/en
Publication of EP1679308A4 publication Critical patent/EP1679308A4/en
Application granted granted Critical
Publication of EP1679308B1 publication Critical patent/EP1679308B1/en
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

To prepare a novel indazole derivative useful as a medicine and to find out a new pharmacological activity of the derivative. The compound is represented by the general formula [I] and has excellent Rho-kinase inhibitory activity. In the formula, ring X is a benzene ring or pyridine ring; R1 and R2 each is hydrogen or alkyl; R3 and R4 each is halogeno, hydrogen, OH, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, cycloalkenyloxy, aryloxy, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, carboxy, hydrocarbonyl, alkylcarbonyl, etc.; and R5 is halogeno, hydrogen, OH, alkoxy, aryloxy, alkyl, or aryl. These groups may be substituted.
EP04792805.6A 2003-10-15 2004-10-15 Novel indazole derivative Not-in-force EP1679308B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP12160543.0A EP2468729B1 (en) 2003-10-15 2004-10-15 Novel indazole derivative

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2003354917 2003-10-15
JP2004270561 2004-08-20
PCT/JP2004/015663 WO2005035506A1 (en) 2003-10-15 2004-10-15 Novel indazole derivative

Related Child Applications (1)

Application Number Title Priority Date Filing Date
EP12160543.0 Division-Into 2012-03-21

Publications (3)

Publication Number Publication Date
EP1679308A1 EP1679308A1 (en) 2006-07-12
EP1679308A4 true EP1679308A4 (en) 2009-06-03
EP1679308B1 EP1679308B1 (en) 2013-07-24

Family

ID=34436941

Family Applications (2)

Application Number Title Priority Date Filing Date
EP12160543.0A Not-in-force EP2468729B1 (en) 2003-10-15 2004-10-15 Novel indazole derivative
EP04792805.6A Not-in-force EP1679308B1 (en) 2003-10-15 2004-10-15 Novel indazole derivative

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP12160543.0A Not-in-force EP2468729B1 (en) 2003-10-15 2004-10-15 Novel indazole derivative

Country Status (9)

Country Link
US (3) US7563906B2 (en)
EP (2) EP2468729B1 (en)
JP (2) JP4110324B2 (en)
KR (1) KR101163800B1 (en)
CN (1) CN1863779B (en)
CA (1) CA2542609C (en)
ES (1) ES2426288T3 (en)
TW (1) TWI344961B (en)
WO (1) WO2005035506A1 (en)

Families Citing this family (97)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI344961B (en) * 2003-10-15 2011-07-11 Ube Industries Novel indazole derivative
NZ547696A (en) 2003-12-23 2009-12-24 Astex Therapeutics Ltd Pyrazole derivatives as protein kinase modulators
EP1784175A4 (en) 2004-08-23 2009-07-22 Merck & Co Inc Inhibitors of akt activity
US20090029970A1 (en) * 2005-02-16 2009-01-29 Astellas Pharma Inc. Pain remedy containing rock inhibitor
RU2414904C2 (en) 2005-03-31 2011-03-27 Асахи Гласс Компани, Лимитед PROTECTIVE MEDICIATION FOR RETINA NEURON WHICH CONTAINS AS ACTIVE COMPONETS PROSTAGLANDIN F2α DERIVATIVE
RU2392938C2 (en) * 2005-04-13 2010-06-27 Убе Индастриз, Лтд Protective agent for neural retina cells containing indazole derivatives as active ingredient
ES2393768T3 (en) * 2005-05-26 2012-12-27 Neuron Systems, Inc Quinoline derivative for the treatment of retinal diseases
US8008317B2 (en) 2005-06-10 2011-08-30 Merck Sharp & Dohme Corp. Inhibitors of akt activtiy
WO2006137368A1 (en) 2005-06-21 2006-12-28 Kowa Co., Ltd. Preventive or remedy for glaucoma
US8343953B2 (en) 2005-06-22 2013-01-01 Astex Therapeutics Limited Pharmaceutical compounds
EP1933832A2 (en) 2005-06-23 2008-06-25 Astex Therapeutics Limited Pharmaceutical combinations comprising pyrazole derivatives as protein kinase modulators
EP1910297B1 (en) 2005-07-11 2016-05-25 Aerie Pharmaceuticals, Inc. Isoquinoline compounds
US20070135499A1 (en) * 2005-07-11 2007-06-14 Aerie Pharmaceuticals, Inc. Hydrazide compounds
PL1905452T3 (en) 2005-07-12 2013-11-29 Kowa Co Agent for prevention or treatment of glaucoma
EP1932841B1 (en) 2005-08-30 2014-01-01 Asahi Kasei Pharma Corporation Sulfonamide compound
KR20080040027A (en) 2005-09-02 2008-05-07 아스테라스 세이야쿠 가부시키가이샤 Amide derivatives as rock inhibitors
US8008481B2 (en) * 2006-03-31 2011-08-30 Ericsson Anna M Indazole compounds
EP2025676A4 (en) * 2006-06-08 2011-06-15 Ube Industries Novel indazole derivative having spiro ring structure in side chain
WO2008036540A2 (en) 2006-09-20 2008-03-27 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
AR064010A1 (en) 2006-12-06 2009-03-04 Merck & Co Inc AKT ACTIVITY INHIBITORS
US20100022517A1 (en) * 2006-12-18 2010-01-28 Richards Lori A Ophthalmic formulation of rho kinase inhibitor compound
US8455513B2 (en) 2007-01-10 2013-06-04 Aerie Pharmaceuticals, Inc. 6-aminoisoquinoline compounds
DE102007002717A1 (en) 2007-01-18 2008-07-24 Merck Patent Gmbh Heterocyclic indazole derivatives
US8415372B2 (en) 2007-02-27 2013-04-09 Asahi Kasei Pharma Corporation Sulfonamide compound
EP2130828A4 (en) 2007-02-28 2010-12-29 Asahi Kasei Pharma Corp Sulfonamide derivative
GB0704932D0 (en) 2007-03-14 2007-04-25 Astex Therapeutics Ltd Pharmaceutical compounds
CA2685529A1 (en) * 2007-04-30 2008-11-06 Abbott Laboratories Inhibitors of diacylglycerol o-acyltransferase type 1 enzyme
DE102007022565A1 (en) 2007-05-14 2008-11-20 Merck Patent Gmbh Heterocyclic indazole derivatives
JP5234825B2 (en) 2007-07-02 2013-07-10 旭化成ファーマ株式会社 Sulfonamide compounds and crystals thereof
SI2178870T1 (en) * 2007-08-17 2018-11-30 Lg Chem, Ltd. Indole and indazole compounds as an inhibitor of cellular necrosis
KR20100080514A (en) 2007-08-29 2010-07-08 센주 세이야꾸 가부시키가이샤 Agent for promoting corneal endothelial cell adhesion
JP5348725B2 (en) * 2007-10-25 2013-11-20 ジェネンテック, インコーポレイテッド Method for producing thienopyrimidine compound
US8455514B2 (en) * 2008-01-17 2013-06-04 Aerie Pharmaceuticals, Inc. 6-and 7-amino isoquinoline compounds and methods for making and using the same
MX2010010471A (en) 2008-03-26 2010-10-20 Daiichi Sankyo Co Ltd Novel tetrahydroisoquinoline derivative.
US8536169B2 (en) 2008-06-05 2013-09-17 Glaxo Group Limited Compounds
WO2009147188A1 (en) 2008-06-05 2009-12-10 Glaxo Group Limited Benzpyrazol derivatives as inhibitors of pi3 kinases
ES2566339T3 (en) * 2008-06-05 2016-04-12 Glaxo Group Limited 4-Carboxamide indazole derivatives useful as PI3-kinase inhibitors
ES2383246T3 (en) 2008-06-05 2012-06-19 Glaxo Group Limited 4-amino-indazoles
EP2299820A4 (en) * 2008-06-18 2012-11-14 Inspire Pharmaceuticals Inc Ophthalmic formulation of rho kinase inhibitor compound
US8450344B2 (en) 2008-07-25 2013-05-28 Aerie Pharmaceuticals, Inc. Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds
WO2010032875A2 (en) * 2008-09-18 2010-03-25 Astellas Pharma Inc. Heterocyclic carboxamide compounds
UY32251A (en) * 2008-11-20 2010-05-31 Glaxosmithkline Llc CHEMICAL COMPOUNDS
WO2010065782A1 (en) * 2008-12-04 2010-06-10 Inspire Pharmaceuticals, Inc. Method for treating pulmonary diseases using rho kinase inhibitor compounds
WO2010102958A1 (en) 2009-03-09 2010-09-16 Glaxo Group Limited 4-oxadiazol-2 -yl- indazoles as inhibitors of p13 kinases
WO2010120854A1 (en) * 2009-04-15 2010-10-21 Glaxosmithkline Llc Chemical compounds
BRPI1016219B8 (en) 2009-04-30 2021-05-25 Glaxo Group Ltd indazole compound substituted with oxazole, and pharmaceutical composition
EP3354643B1 (en) 2009-05-01 2020-10-28 Aerie Pharmaceuticals, Inc. Dual mechanism inhibitors for the treatment of disease
EP2488630B1 (en) 2009-10-16 2017-07-05 The Scripps Research Institute Induction of pluripotent cells
JP5885670B2 (en) 2009-12-11 2016-03-15 アルデイラ セラピューティクス, インコーポレイテッド Compositions and methods for the treatment of macular degeneration
EP2569301A1 (en) 2010-05-12 2013-03-20 Abbvie Inc. Indazole inhibitors of kinase
TWI476188B (en) * 2010-05-27 2015-03-11 Ube Industries Novel indazole derivative or salt thereof and production intermediate thereof, and antioxidant using same
TW201202214A (en) * 2010-05-27 2012-01-16 Santen Pharmaceutical Co Ltd Novel indazole derivative or salt thereof, production intermediate thereof, and prophylactic or therapeutic agent for chorioretinal degeneratire disease using the same
GB201018124D0 (en) 2010-10-27 2010-12-08 Glaxo Group Ltd Polymorphs and salts
AU2011349446C1 (en) 2010-12-22 2016-01-21 Fate Therapauetics, Inc. Cell culture platform for single cell sorting and enhanced reprogramming of iPSCs
CN102675286B (en) * 2011-03-07 2015-08-19 中国科学院上海药物研究所 One class indazole compounds and preparation method thereof, purposes and pharmaceutical composition
PT2788472T (en) 2011-12-06 2019-04-01 Astellas Inst For Regenerative Medicine Method of directed differentiation producing corneal endothelial cells, compositions thereof, and uses thereof
ES2917222T3 (en) 2011-12-28 2022-07-07 Kyoto Prefectural Public Univ Corp Normalization of corneal endothelial cell culture
EP2628482A1 (en) 2012-02-17 2013-08-21 Academisch Medisch Centrum Rho kinase inhiitors for use in the treatment of neuroblastoma
US8889730B2 (en) 2012-04-10 2014-11-18 Pfizer Inc. Indole and indazole compounds that activate AMPK
EP2935220A4 (en) 2012-12-20 2016-04-27 Aldeyra Therapeutics Inc Peri-carbinols
RU2018145691A (en) 2013-01-23 2019-04-01 Альдейра Терапьютикс, Инк. DISEASES ASSOCIATED WITH TOXIC ALDEHYDE AND THEIR TREATMENT
AU2014209585A1 (en) 2013-01-25 2015-07-23 Aldeyra Therapeutics, Inc. Novel traps in the treatment of macular degeneration
EP2970177A1 (en) 2013-03-15 2016-01-20 Pfizer Inc. Indole compounds that activate ampk
US20140275160A1 (en) 2013-03-15 2014-09-18 Aerie Pharmaceuticals, Inc. Combination therapy
WO2015016371A1 (en) 2013-07-30 2015-02-05 京都府公立大学法人 Corneal endothelial cell marker
EP3064222B1 (en) 2013-10-31 2020-10-21 Kyoto Prefectural Public University Corporation Therapeutic drug comprising tgf-beta signal inhibitor for diseases related to endoplasmic reticulum cell death in corneal endothelium
RU2704984C1 (en) 2013-11-27 2019-11-01 Киото Прифекчурал Паблик Юниверсити Корпорэйшн Using laminin in corneal endothelial cell culture
EP3604499A1 (en) 2014-03-04 2020-02-05 Fate Therapeutics, Inc. Improved reprogramming methods and cell culture platforms
GB201511382D0 (en) 2015-06-29 2015-08-12 Imp Innovations Ltd Novel compounds and their use in therapy
AU2016311158A1 (en) 2015-08-21 2018-04-05 Aldeyra Therapeutics, Inc. Deuterated compounds and uses thereof
US20180296474A1 (en) 2015-10-13 2018-10-18 INSERM (Institut National de la Santé et de la Recherche Médicale Methods and pharmaceutical compositions for the treatment of retinal capillary non-perfusion
EP4088719A1 (en) 2015-10-13 2022-11-16 Institut National de la Santé et de la Recherche Médicale (INSERM) Methods and pharmaceutical compositions for the treatment of retinal capillary non-perfusion
CA3001917A1 (en) 2015-10-16 2017-04-20 Fate Therapeutics, Inc. Platform for the induction & maintenance of ground state pluripotency
US9643927B1 (en) 2015-11-17 2017-05-09 Aerie Pharmaceuticals, Inc. Process for the preparation of kinase inhibitors and intermediates thereof
EP3376870B1 (en) 2015-11-17 2021-08-11 Aerie Pharmaceuticals, Inc. Process for the preparation of kinase inhibitors and intermediates thereof
US20190083543A1 (en) 2016-02-15 2019-03-21 Kyoto Prefectural Public University Corporation Human functional corneal endothelial cell and application thereof
US11129823B2 (en) 2016-05-09 2021-09-28 Aldeyra Therapeutics, Inc. Combination treatment of ocular inflammatory disorders and diseases
KR102568079B1 (en) 2016-08-31 2023-08-17 에어리 파마슈티컬즈, 인코포레이티드 Ophthalmic compositions
US20210130339A1 (en) * 2017-01-25 2021-05-06 Glaxosmithkline Intellectual Property Development Limited Compounds
BR112019015269A2 (en) * 2017-01-25 2020-04-14 Glaxosmithkline Ip Dev Ltd compounds
WO2018170476A1 (en) 2017-03-16 2018-09-20 Aldeyra Therapeutics, Inc. Polymorphic compounds and uses thereof
KR20190135027A (en) 2017-03-31 2019-12-05 에어리 파마슈티컬즈, 인코포레이티드 Aryl Cyclopropyl-amino-isoquinolinyl Amide Compound
CN110944668A (en) 2017-06-16 2020-03-31 学校法人同志社 Medicament comprising an mTOR inhibitor for treating or preventing ocular symptoms, disorders or diseases and uses thereof
US20200121652A1 (en) 2017-06-16 2020-04-23 The Doshisha Compounds having caspase inhibitory activity, pharmaceutical agent containing said compounds and for treating or preventing corneal endothelial symptoms, disorders, or diseases, and application of said pharmaceutical agent
AU2018348174A1 (en) 2017-10-10 2020-04-23 Aldeyra Therapeutics, Inc. Treatment of inflammatory disorders
CA3082643A1 (en) 2017-11-14 2019-05-23 The Schepens Eye Research Institute, Inc. Runx1 inhibition for treatment of proliferative vitreoretinopathy and conditions associated with epithelial to mesenchymal transition
CN110452176A (en) * 2018-05-07 2019-11-15 四川大学 Indazole analog derivative and its preparation method and application
EP3833660A4 (en) 2018-08-06 2022-05-11 Aldeyra Therapeutics, Inc. Polymorphic compounds and uses thereof
EP3843845A4 (en) 2018-08-29 2022-05-11 University Of Massachusetts Inhibition of protein kinases to treat friedreich ataxia
US20210207088A1 (en) 2018-08-31 2021-07-08 The Doshisha Composition and method for preserving or culturing ocular cells
WO2020056345A1 (en) 2018-09-14 2020-03-19 Aerie Pharmaceuticals, Inc. Aryl cyclopropyl-amino-isoquinolinyl amide compounds
KR20210069640A (en) 2018-10-02 2021-06-11 학교법인 도시샤 Methods and Vessels for Preserving Corneal Endothelial Cells
WO2020193802A1 (en) 2019-03-28 2020-10-01 Fundación De La Comunidad Valenciana Centro De Investigación Príncipe Felipe Polymeric conjugates and uses thereof
CN110483403A (en) * 2019-09-02 2019-11-22 南通大学 A kind of synthetic method of the bromo- 4- methoxyl group -1H- indazole of 5-
KR20220146552A (en) 2020-02-27 2022-11-01 교토후고리츠다이가쿠호진 Human functional corneal endothelial cells and their applications
BR112023003807A2 (en) 2020-09-18 2023-03-28 Sumitomo Pharma Co Ltd AMINE DERIVATIVE
WO2022235586A1 (en) 2021-05-03 2022-11-10 Astellas Institute For Regenerative Medicine Methods of generating mature corneal endothelial cells

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4022900A (en) * 1970-09-09 1977-05-10 Marion Laboratories, Inc. Compositions containing 1,2,3,4-tetrahydroisoquinolines used as hypotensive agents
KR100452715B1 (en) 1995-12-21 2004-12-17 알콘 래보레이토리스, 인코퍼레이티드 Use of certain isoquinolinesulfonyl compounds for the treatment of glaucoma and ischemia
US6586425B2 (en) * 1996-02-21 2003-07-01 Wisconsin Alumni Research Foundation Cytoskeletal active agents for glaucoma therapy
US5798380A (en) * 1996-02-21 1998-08-25 Wisconsin Alumni Research Foundation Cytoskeletal active agents for glaucoma therapy
US6218410B1 (en) 1996-08-12 2001-04-17 Yoshitomi Pharmaceutical Industries, Ltd. Medicines comprising Rho kinase inhibitor
JP4212149B2 (en) 1998-06-11 2009-01-21 株式会社デ・ウエスタン・セラピテクス研究所 Medicine
US20020061846A1 (en) 2000-02-02 2002-05-23 Hellerqvist Carl G. Methods for preventing or attenuating pathoangiogenic conditions
WO2000009162A1 (en) 1998-08-17 2000-02-24 Senju Pharmaceutical Co., Ltd. Preventives/remedies for glaucoma
AU3328600A (en) 1999-03-25 2000-10-16 Santen Pharmaceutical Co. Ltd. Ocular tension-lowering agents
YU54202A (en) * 2000-01-18 2006-01-16 Agouron Pharmaceuticals Inc. Indazole compounds,pharmaceutical compositions,and methods for mediating or inhibiting cell proliferation
US7217722B2 (en) * 2000-02-01 2007-05-15 Kirin Beer Kabushiki Kaisha Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
PT1370553E (en) 2001-03-23 2006-09-29 Bayer Corp RHOQUINASE INHIBITORS
AU2002245709A1 (en) 2001-03-23 2002-10-08 Bayer Corporation Rho-kinase inhibitors
US7199147B2 (en) 2001-06-12 2007-04-03 Dainippon Sumitomo Pharma Co., Ltd. Rho kinase inhibitors
US6718759B1 (en) 2002-09-25 2004-04-13 Husco International, Inc. Velocity based method for controlling a hydraulic system
TWI344961B (en) * 2003-10-15 2011-07-11 Ube Industries Novel indazole derivative

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
No further relevant documents disclosed *

Also Published As

Publication number Publication date
CA2542609A1 (en) 2005-04-21
KR20060128857A (en) 2006-12-14
US20090264468A1 (en) 2009-10-22
US20110039891A1 (en) 2011-02-17
EP1679308B1 (en) 2013-07-24
TWI344961B (en) 2011-07-11
EP2468729A1 (en) 2012-06-27
ES2426288T3 (en) 2013-10-22
US7855222B2 (en) 2010-12-21
CA2542609C (en) 2013-06-04
KR101163800B1 (en) 2012-07-09
JP4922955B2 (en) 2012-04-25
WO2005035506A1 (en) 2005-04-21
US20070129404A1 (en) 2007-06-07
JPWO2005035506A1 (en) 2007-04-19
EP1679308A1 (en) 2006-07-12
CN1863779A (en) 2006-11-15
CN1863779B (en) 2010-05-05
JP4110324B2 (en) 2008-07-02
EP2468729B1 (en) 2013-12-25
US7563906B2 (en) 2009-07-21
US8232308B2 (en) 2012-07-31
JP2008143913A (en) 2008-06-26
TW200524896A (en) 2005-08-01

Similar Documents

Publication Publication Date Title
EP1679308A4 (en) Novel indazole derivative
TW200745034A (en) New compounds
TW200800988A (en) Polycyclic carbamoylpyridone derivative having HIV integrase inhibitory activity
MX9709951A (en) Benzamide derivatives and their use as vasopressin antagonists.
WO2010017055A3 (en) Dihydropyridophthalazinone inhibitors of poly(adp-ribose)polymerase (parp)
WO2004058679A3 (en) Ligands of adenine nucleotide translocase (ant) and compositions and methods related thereto
CA2286723A1 (en) Tricyclic compounds
MXPA03009497A (en) 2-iminopyrrolidine derivatives.
MX2009006397A (en) Imidazothiazole derivatives.
MXPA04006322A (en) 6-fluorobicyclo[3.1.0]hexane derivatives.
ZA200609634B (en) Quinazolinone derivatives useful as vanilloid antagonists
TW200626598A (en) Pyrrazolo-pyrimidine derivatives
WO2008078725A1 (en) Thiazepine derivative
EP1726584A4 (en) 2-aminoquinazoline derivative
WO2007033039A3 (en) Proteasome inhibiting beta lactam compounds
AU2267495A (en) Benzamide derivatives as vasopressin antagonists
EP1300399A4 (en) Phenylpyridazine derivatives and drugs containing the same
WO2008105526A1 (en) Macrocyclic compound
TN2011000265A1 (en) Rifamycin derivatives
WO2003024953A1 (en) Propanolamine derivative having 1,4-benzodioxane ring
MXPA05011962A (en) Substituted oxyarenes, and use thereof for controlling pests.
TN2010000173A1 (en) CGRP ANTAGONISTS
WO2008111632A1 (en) Glucocorticoid receptor agonist composed of 2,2,4-trimethyl-6-phenyl-1,2-dihydroquinoline derivative
WO2003057671A1 (en) Biaryl compound and use thereof
MY161992A (en) Novel tetrahydroisoquinoline derivative

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20060509

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20090504

17Q First examination report despatched

Effective date: 20100916

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602004042850

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: C07D0231560000

Ipc: C07D0403040000

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: UBE INDUSTRIES, LTD.

RIC1 Information provided on ipc code assigned before grant

Ipc: A61P 43/00 20060101ALI20130121BHEP

Ipc: C07D 401/04 20060101ALI20130121BHEP

Ipc: C07D 413/04 20060101ALI20130121BHEP

Ipc: A61K 31/4439 20060101ALI20130121BHEP

Ipc: A61K 31/416 20060101ALI20130121BHEP

Ipc: C07D 231/56 20060101ALI20130121BHEP

Ipc: A61P 27/06 20060101ALI20130121BHEP

Ipc: C07D 403/04 20060101AFI20130121BHEP

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 623366

Country of ref document: AT

Kind code of ref document: T

Effective date: 20130815

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602004042850

Country of ref document: DE

Effective date: 20130919

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2426288

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20131022

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 623366

Country of ref document: AT

Kind code of ref document: T

Effective date: 20130724

REG Reference to a national code

Ref country code: NL

Ref legal event code: VDEP

Effective date: 20130724

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130710

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20131125

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20131025

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20140425

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20131031

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20131031

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602004042850

Country of ref document: DE

Effective date: 20140425

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20131015

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20131015

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130724

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20041015

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20150915

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20150908

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20151006

Year of fee payment: 12

Ref country code: GB

Payment date: 20151014

Year of fee payment: 12

Ref country code: IT

Payment date: 20151026

Year of fee payment: 12

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602004042850

Country of ref document: DE

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20161015

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20170630

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20161015

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170503

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20161102

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20161015

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20161016

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20181123